Canonical Allele Identifier: CA1989919890

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178284A= , CM000673.2:g.89178284A=	GRCh38
NC_000011.9:g.88911452A= , CM000673.1:g.88911452A=	GRCh37
NC_000011.8:g.88551100A=	NCBI36
NG_008748.1:g.5413A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.331A= MANE Select	ENSP00000263321.4:p.Asn111=
ENST00000263321.5:c.331A=	ENSP00000263321.4:p.Asn111=
ENST00000526139.1:n.392A=
NM_000372.4:c.331A=	NP_000363.1:p.Asn111=
XM_011542970.1:c.331A=	XP_011541272.1:p.Asn111=
XM_011542970.2:c.331A=	XP_011541272.1:p.Asn111=
XR_001748321.1:n.2718-64751T=
XR_001748322.1:n.2733-64751T=
NM_000372.5:c.331A= MANE Select	NP_000363.1:p.Asn111=